BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 20470418)

  • 1. SCN5A allelic expression imbalance in African-Americans heterozygous for the common variant p.Ser1103Tyr.
    Killen SA; Kunic J; Wang L; Lewis A; Levy BP; Ackerman MJ; George AL
    BMC Med Genet; 2010 May; 11():74. PubMed ID: 20470418
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndrome.
    Van Norstrand DW; Tester DJ; Ackerman MJ
    Heart Rhythm; 2008 May; 5(5):712-5. PubMed ID: 18452875
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y.
    Plant LD; Bowers PN; Liu Q; Morgan T; Zhang T; State MW; Chen W; Kittles RA; Goldstein SA
    J Clin Invest; 2006 Feb; 116(2):430-5. PubMed ID: 16453024
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Analysis of PAC1 receptor gene variants in Caucasian and African American infants dying of sudden infant death syndrome.
    Barrett KT; Rodikova E; Weese-Mayer DE; Rand CM; Marazita ML; Cooper ME; Berry-Kravis EM; Bech-Hansen NT; Wilson RJ
    Acta Paediatr; 2013 Dec; 102(12):e546-52. PubMed ID: 23981011
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP).
    Cummings KJ; Klotz C; Liu WQ; Weese-Mayer DE; Marazita ML; Cooper ME; Berry-Kravis EM; Tobias R; Goldie C; Bech-Hansen NT; Wilson RJ
    Acta Paediatr; 2009 Mar; 98(3):482-9. PubMed ID: 19120039
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association of the serotonin transporter gene with sudden infant death syndrome: a haplotype analysis.
    Weese-Mayer DE; Zhou L; Berry-Kravis EM; Maher BS; Silvestri JM; Marazita ML
    Am J Med Genet A; 2003 Oct; 122A(3):238-45. PubMed ID: 12966525
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Serotonin-related FEV gene variant in the sudden infant death syndrome is a common polymorphism in the African-American population.
    Broadbelt KG; Barger MA; Paterson DS; Holm IA; Haas EA; Krous HF; Kinney HC; Markianos K; Beggs AH
    Pediatr Res; 2009 Dec; 66(6):631-5. PubMed ID: 19707175
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The contribution of prone sleeping position to the racial disparity in sudden infant death syndrome: the Chicago Infant Mortality Study.
    Hauck FR; Moore CM; Herman SM; Donovan M; Kalelkar M; Christoffel KK; Hoffman HJ; Rowley D
    Pediatrics; 2002 Oct; 110(4):772-80. PubMed ID: 12359794
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sudden infant death syndrome: rare mutation in the serotonin system FEV gene.
    Rand CM; Berry-Kravis EM; Zhou L; Fan W; Weese-Mayer DE
    Pediatr Res; 2007 Aug; 62(2):180-2. PubMed ID: 17597646
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The common African American polymorphism SCN5A-S1103Y interacts with mutation SCN5A-R680H to increase late Na current.
    Cheng J; Tester DJ; Tan BH; Valdivia CR; Kroboth S; Ye B; January CT; Ackerman MJ; Makielski JC
    Physiol Genomics; 2011 May; 43(9):461-6. PubMed ID: 21385947
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data.
    Andreasen C; Refsgaard L; Nielsen JB; Sajadieh A; Winkel BG; Tfelt-Hansen J; Haunsø S; Holst AG; Svendsen JH; Olesen MS
    Can J Cardiol; 2013 Sep; 29(9):1104-9. PubMed ID: 23465283
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Postmortem molecular analysis of SCN5A defects in sudden infant death syndrome.
    Ackerman MJ; Siu BL; Sturner WQ; Tester DJ; Valdivia CR; Makielski JC; Towbin JA
    JAMA; 2001 Nov; 286(18):2264-9. PubMed ID: 11710892
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Apolipoprotein E e4 and its prevalence in early childhood death due to sudden infant death syndrome or to recognised causes.
    Becher JC; Keeling JW; Bell J; Wyatt B; McIntosh N
    Early Hum Dev; 2008 Aug; 84(8):549-54. PubMed ID: 18280677
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sudden infant death syndrome: association with a promoter polymorphism of the serotonin transporter gene.
    Weese-Mayer DE; Berry-Kravis EM; Maher BS; Silvestri JM; Curran ME; Marazita ML
    Am J Med Genet A; 2003 Mar; 117A(3):268-74. PubMed ID: 12599191
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Racial disparity and modifiable risk factors among infants dying suddenly and unexpectedly.
    Unger B; Kemp JS; Wilkins D; Psara R; Ledbetter T; Graham M; Case M; Thach BT
    Pediatrics; 2003 Feb; 111(2):E127-31. PubMed ID: 12563085
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cardiac Genetic Predisposition in Sudden Infant Death Syndrome.
    Tester DJ; Wong LCH; Chanana P; Jaye A; Evans JM; FitzPatrick DR; Evans MJ; Fleming P; Jeffrey I; Cohen MC; Tfelt-Hansen J; Simpson MA; Behr ER; Ackerman MJ
    J Am Coll Cardiol; 2018 Mar; 71(11):1217-1227. PubMed ID: 29544605
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A controlled study of the relationship between Bordetella pertussis infections and sudden unexpected deaths among German infants.
    Heininger U; Kleemann WJ; Cherry JD;
    Pediatrics; 2004 Jul; 114(1):e9-15. PubMed ID: 15231967
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Patient-specific, re-engineered cardiomyocyte model confirms the circumstance-dependent arrhythmia risk associated with the African-specific common SCN5A polymorphism p.S1103Y: Implications for the increased sudden deaths observed in black individuals during the COVID-19 pandemic.
    Hamrick SK; John Kim CS; Tester DJ; Giudicessi JR; Ackerman MJ
    Heart Rhythm; 2022 May; 19(5):822-827. PubMed ID: 34979239
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The sudden infant death syndrome gene: does it exist?
    Opdal SH; Rognum TO
    Pediatrics; 2004 Oct; 114(4):e506-12. PubMed ID: 15466077
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channels.
    Makielski JC; Ye B; Valdivia CR; Pagel MD; Pu J; Tester DJ; Ackerman MJ
    Circ Res; 2003 Oct; 93(9):821-8. PubMed ID: 14500339
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.